Legal

At Sleep Easy Tech, our product is unique and innovative, and there is tremendous excitement from consumers experience with our products. It is important to remember, however, that marketing claims not in harmony with applicable laws could jeopardize your ability to continue to successfully market these innovative products.

The Oxyllow® System is a Class I 510K Exempt Medical Device. It does not require 510K Pre-Market submission, and therefore, has not been evaluated by the FDA. Individual results from using the Oxyllow® System with oxygen therapy require proper use. Claims that the Oxyllow® System is approved by the FDA or any other government agency are false and strictly prohibited.

If you have any questions about alternative oxygen therapy products, or if the Oxyllow® System is a good option for you, consult your doctor/healthcare provider.